Canonical Allele Identifier: CA2579836369

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127401149C>G , CM000670.2:g.127401149C>G GRCh38
NC_000008.10:g.128413394C>G , CM000670.1:g.128413394C>G GRCh37
NC_000008.9:g.128482576C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000645438.1:c.-559-13739C>G (POU5F1B) ENSP00000495779.1:n.-559-13739C>G
NR_109834.1:n.751C>G (CCAT2)
NR_117100.1:n.1176+19680G>C (CASC8)